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Results of search for 'au:"Simon, D B"', page 2 of 2
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Authors
Achard, J M
Al-Sabban, E
Alkhnbashi, Omer S
Alpay, H
Backofen, Rolf
Bia, M J
Choate, K A
Cruz, D N
DiPietro, A
Farfel, Z
Karet, F E
Lifton, R P
Mansfield, T A
Mayan, H
Nelson-Williams, C
Ringel, S P
Rodriguez-Soriano, J
Sanjad, S A
Simon, D B
Trachtman, H
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Topics
Adult
Alkalosis
Amino Acid Sequence
Animals
Bartter Syndrome
Base Sequence
Carrier Proteins
Female
Genetic Linkage
Humans
Male
Middle Aged
Molecular Sequence Data
Mutation
Pedigree
Sodium-Potassium-Chloride Symporters
Syndrome
chemistry
genetics
metabolism
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Your search returned 22 results.
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21.
Human hypertension caused by mutations in WNK kinases.
[electronic resource]
by
Wilson, F H
Disse-Nicodème, S
Choate, K A
Ishikawa, K
Nelson-Williams, C
Desitter, I
Gunel, M
Milford, D V
Lipkin, G W
Achard, J M
Feely, M P
Dussol, B
Berland, Y
Unwin, R J
Mayan, H
Simon, D B
Farfel, Z
Jeunemaitre, X
Lifton, R P
Producer:
20010906
In:
Science (New York, N.Y.)
vol. 293
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22.
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.
[electronic resource]
by
Simon, D B
Bindra, R S
Mansfield, T A
Nelson-Williams, C
Mendonca, E
Stone, R
Schurman, S
Nayir, A
Alpay, H
Bakkaloglu, A
Rodriguez-Soriano, J
Morales, J M
Sanjad, S A
Taylor, C M
Pilz, D
Brem, A
Trachtman, H
Griswold, W
Richard, G A
John, E
Lifton, R P
Producer:
19971114
In:
Nature genetics
vol. 17
Online resources:
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